Portal Access, Inc.
Country not established
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
FLEXI-PORT™ Power Injectable Implantable Port Ref K260916
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 119535395
Frequently asked questions
How many devices does Portal Access, Inc. have in the registry?
The registry currently lists 5 devices for Portal Access, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Portal Access, Inc.'s devices?
Among its 5 most recently registered devices, Portal Access, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Portal Access, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Portal Access, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Portal Access, Inc. in the registry?
The most recently registered devices listed for Portal Access, Inc. include FLEXI-PORT 68362, FLEXI-PORT 68360, FLEXI-PORT 68364 and FLEXI-PORT 68363.